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转录因子 NRF2 对大麻素 CB 受体的调节在小胶质细胞中具有特异性。

Cannabinoid CB Receptor Modulation by the Transcription Factor NRF2 is Specific in Microglial Cells.

机构信息

Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Instituto de Investigación Sanitaria La Paz (IdiPaz), Instituto de Investigaciones Biomédicas "Alberto Sols", UAM-CSIC, C/Arturo Duperier, 4, 28029, Madrid, Spain.

Department of Biochemistry, School of Medicine, Universidad Autónoma de Madrid, Madrid, Spain.

出版信息

Cell Mol Neurobiol. 2020 Jan;40(1):167-177. doi: 10.1007/s10571-019-00719-y. Epub 2019 Aug 5.

Abstract

Nuclear factor erythroid 2-related factor 2 (NRF2) is a pleiotropic transcription factor that has neuroprotective and anti-inflammatory effects, regulating more than 250 genes. As NRF2, cannabinoid receptor type 2 (CB) is also implicated in the preservation of neurons against glia-driven inflammation. To this concern, little is known about the regulation pathways implicated in CB receptor expression. In this study, we analyze whether NRF2 could modulate the transcription of CB in neuronal and microglial cells. Bioinformatics analysis revealed an antioxidant response element in the promoter sequence of the CB receptor gene. Further analysis by chemical and genetic manipulations of this transcription factor demonstrated that NRF2 is not able to modulate the expression of CB in neurons. On the other hand, at the level of microglia, the expression of CB is NRF2-dependent. These results are related to the differential levels of expression of both genes regarding the brain cell type. Since modulation of CB receptor signaling may represent a promising therapeutic target with minimal psychotropic effects that can be used to modulate endocannabinoid-based therapeutic approaches and to reduce neurodegeneration, our findings will contribute to disclose the potential of CB as a novel target for treating different pathologies.

摘要

核因子红细胞 2 相关因子 2(NRF2)是一种多效性转录因子,具有神经保护和抗炎作用,可调节超过 250 个基因。作为 NRF2,大麻素受体 2(CB)也与神经元对抗胶质细胞驱动的炎症的保护有关。关于这一点,人们对涉及 CB 受体表达的调节途径知之甚少。在这项研究中,我们分析了 NRF2 是否可以调节神经元和小胶质细胞中 CB 的转录。生物信息学分析显示 CB 受体基因启动子序列中存在抗氧化反应元件。通过对该转录因子进行化学和遗传操作的进一步分析表明,NRF2 不能调节神经元中 CB 的表达。另一方面,在小胶质细胞水平上,CB 的表达依赖于 NRF2。这些结果与两种基因在脑细胞类型方面的表达水平差异有关。由于 CB 受体信号的调节可能代表一种有前途的治疗靶点,其具有最小的精神作用,可以用于调节内源性大麻素为基础的治疗方法并减少神经退行性变,因此我们的研究结果将有助于揭示 CB 作为治疗不同疾病的新靶标的潜力。

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